A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1099589



Internal ID15952775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:151132928..151196543hg38UCSC Ensembl
Innerchr7:150830015..150893629hg19UCSC Ensembl
Innerchr7:150460948..150524562hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3863616
hg1963615
hg1863615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609034
Supporting Variants
Samples
Known GenesAGAP3, ASB10, GBX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1099589
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer